Version: 8.0.0
Date: Tue Jan 28 2025
6 results
Allele/Variant Genes: BCL2 (Hsa)

(GRCh38)18:63318209A>T

(Homo sapiens)
Allele/Variant
Source: rs2144321951
Genes: BCL2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)18:63318209A>T

(GRCh38)18:63318596G>A

(Homo sapiens)
Allele/Variant
Source: rs1913587435
Genes: BCL2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)18:63318596G>A

(GRCh38)18:63318208G>A

(Homo sapiens)
Allele/Variant
Source: rs137945099
Genes: BCL2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)18:63318208G>A

(GRCh38)18:63318329G>T

(Homo sapiens)
Allele/Variant
Source: rs990629198
Genes: BCL2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)18:63318329G>T

(GRCh38)18:63318367G>A

(Homo sapiens)
Allele/Variant
Source: rs61733416
Genes: BCL2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)18:63318367G>A

(GRCh38)18:63318646T>C

(Homo sapiens)
Allele/Variant
Source: rs1801018
Genes: BCL2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)18:63318646T>C